The diagnostic value of nasal microbiota and clinical parameters in a multi-parametric prediction model to differentiate bacterial versus viral infections in lower respiratory tract infections

Author:

Li YunleiORCID,van Houten Chantal B.,Boers Stefan A.,Jansen Ruud,Cohen Asi,Engelhard Dan,Kraaij Robert,Hiltemann Saskia D.,Ju Jie,Fernández David,Mankoc Cristian,González Eva,de Waal Wouter J.,de Winter-de Groot Karin M.,Wolfs Tom F. W.,Meijers Pieter,Luijk Bart,Oosterheert Jan Jelrik,Sankatsing Sanjay U. C.,Bossink Aik W. J.,Stein Michal,Klein Adi,Ashkar Jalal,Bamberger Ellen,Srugo Isaac,Odeh Majed,Dotan Yaniv,Boico Olga,Etshtein Liat,Paz Meital,Navon Roy,Friedman Tom,Simon Einav,Gottlieb Tanya M.,Pri-Or Ester,Kronenfeld Gali,Oved KfirORCID,Eden Eran,Stubbs Andrew P.,Bont Louis J.,Hays John P.

Abstract

Background The ability to accurately distinguish bacterial from viral infection would help clinicians better target antimicrobial therapy during suspected lower respiratory tract infections (LRTI). Although technological developments make it feasible to rapidly generate patient-specific microbiota profiles, evidence is required to show the clinical value of using microbiota data for infection diagnosis. In this study, we investigated whether adding nasal cavity microbiota profiles to readily available clinical information could improve machine learning classifiers to distinguish bacterial from viral infection in patients with LRTI. Results Various multi-parametric Random Forests classifiers were evaluated on the clinical and microbiota data of 293 LRTI patients for their prediction accuracies to differentiate bacterial from viral infection. The most predictive variable was C-reactive protein (CRP). We observed a marginal prediction improvement when 7 most prevalent nasal microbiota genera were added to the CRP model. In contrast, adding three clinical variables, absolute neutrophil count, consolidation on X-ray, and age group to the CRP model significantly improved the prediction. The best model correctly predicted 85% of the ‘bacterial’ patients and 82% of the ‘viral’ patients using 13 clinical and 3 nasal cavity microbiota genera (Staphylococcus, Moraxella, and Streptococcus). Conclusions We developed high-accuracy multi-parametric machine learning classifiers to differentiate bacterial from viral infections in LRTI patients of various ages. We demonstrated the predictive value of four easy-to-collect clinical variables which facilitate personalized and accurate clinical decision-making. We observed that nasal cavity microbiota correlate with the clinical variables and thus may not add significant value to diagnostic algorithms that aim to differentiate bacterial from viral infections.

Funder

FP7 Health

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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